JPS5594366A - 4-p-alkyl benzoyloxy-pyridine oxide - Google Patents

4-p-alkyl benzoyloxy-pyridine oxide

Info

Publication number
JPS5594366A
JPS5594366A JP135179A JP135179A JPS5594366A JP S5594366 A JPS5594366 A JP S5594366A JP 135179 A JP135179 A JP 135179A JP 135179 A JP135179 A JP 135179A JP S5594366 A JPS5594366 A JP S5594366A
Authority
JP
Japan
Prior art keywords
formula
compound
oxide
reacted
pyridine oxide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP135179A
Other languages
Japanese (ja)
Other versions
JPS615475B2 (en
Inventor
Kazuhisa Toriyama
Tsujiaki Hata
Shinji Hasegawa
Masaru Sasaki
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hitachi Ltd
Original Assignee
Hitachi Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP135179A priority Critical patent/JPS5594366A/en
Priority to DE3000375A priority patent/DE3000375C2/en
Priority to GB8000425A priority patent/GB2039482B/en
Priority to US06/111,104 priority patent/US4293698A/en
Publication of JPS5594366A publication Critical patent/JPS5594366A/en
Publication of JPS615475B2 publication Critical patent/JPS615475B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/89Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/34Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
    • C09K19/3441Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom
    • C09K19/3444Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom the heterocyclic ring being a six-membered aromatic ring containing one nitrogen atom, e.g. pyridine

Abstract

NEW MATERIAL:A 4-p-alkylbenzoyloxypyridine oxide of formula I (R is 1W9C straight chain alkyl group).
EXAMPLE: 4-p-Methylbenzoyloxypyridine oxide of formula VI.
USE: Compounds for controlling the dielectric constant of nematic liquid crystals, used as photoelectric display elements, preferably in an amount of 5W30mol% based on the total mixture. The threshold voltage can be reduced sharply without changing the transition temperature.
PROCESS: A compound of formula II is reacted with a halogenating agent to give a compound of formula III (X is halogen), which is then reacted with a compound of formula V, obtained by oxidizing the compound of formula IV, to form the objective compound of formula I.
COPYRIGHT: (C)1980,JPO&Japio
JP135179A 1979-01-12 1979-01-12 4-p-alkyl benzoyloxy-pyridine oxide Granted JPS5594366A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP135179A JPS5594366A (en) 1979-01-12 1979-01-12 4-p-alkyl benzoyloxy-pyridine oxide
DE3000375A DE3000375C2 (en) 1979-01-12 1980-01-07 4- (4-n-Alkylbenzoyloxy) pyridine oxides and their use for adjusting the dielectric constants of liquid crystals
GB8000425A GB2039482B (en) 1979-01-12 1980-01-07 4-p-alkyl-benzoyloxypyridine-n-oxides useful for controlling dielectric constant of liquid crystal
US06/111,104 US4293698A (en) 1979-01-12 1980-01-10 Compound for controlling dielectric constant of liquid crystal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP135179A JPS5594366A (en) 1979-01-12 1979-01-12 4-p-alkyl benzoyloxy-pyridine oxide

Publications (2)

Publication Number Publication Date
JPS5594366A true JPS5594366A (en) 1980-07-17
JPS615475B2 JPS615475B2 (en) 1986-02-18

Family

ID=11499061

Family Applications (1)

Application Number Title Priority Date Filing Date
JP135179A Granted JPS5594366A (en) 1979-01-12 1979-01-12 4-p-alkyl benzoyloxy-pyridine oxide

Country Status (4)

Country Link
US (1) US4293698A (en)
JP (1) JPS5594366A (en)
DE (1) DE3000375C2 (en)
GB (1) GB2039482B (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DD245896A1 (en) * 1983-12-22 1987-05-20 Dietrich Demus NEMATIVE LIQUID CRYSTAL MIXTURES
US5145601A (en) * 1990-06-25 1992-09-08 The University Of Colorado Foundation Inc. Ferroelectric liquid crystals with nicotinic acid cores
AU2010308571B2 (en) 2009-10-22 2016-10-13 Tpc-Api Llc Methods of making and using compositions comprising flavonoids
US8637569B2 (en) 2009-10-22 2014-01-28 Api Genesis, Llc Methods of increasing solubility of poorly soluble compounds and methods of making and using formulations of such compounds

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3923857A (en) * 1972-02-23 1975-12-02 Hoffmann La Roche Liquid crystal esters
US3927064A (en) * 1972-02-23 1975-12-16 Hoffmann La Roche Benzylidene-aminobenzonitriles
JPS5043076A (en) * 1973-08-20 1975-04-18
US3983049A (en) * 1974-05-02 1976-09-28 General Electric Company Liquid crystal compositions with positive dielectric anisotropy
CH599333A5 (en) * 1976-05-04 1978-05-31 Bbc Brown Boveri & Cie

Also Published As

Publication number Publication date
US4293698A (en) 1981-10-06
JPS615475B2 (en) 1986-02-18
GB2039482B (en) 1983-02-16
DE3000375A1 (en) 1980-07-24
DE3000375C2 (en) 1982-08-12
GB2039482A (en) 1980-08-13

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